ALCAPA in an adult with preserved left ventricular function. J Card Surg 2003 Jan-Feb;18(1):25-8
Date
04/17/2003Pubmed ID
12696764DOI
10.1046/j.1540-8191.2003.01908.xScopus ID
2-s2.0-0037242620 16 CitationsAbstract
Anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) is the most common congenital coronary artery defect. Left uncorrected, nearly 90% of patients will die within one year. Without surgical repair, surviving patients are subjected to risks of myocardial ischemia with global cardiomyopathy, chronic mitral regurgitation, and sudden death. We report a case of ALCAPA in a 23-year-old female with completely preserved left ventricular function. This article reviews the mechanism of this unusual presentation as well as the therapeutic options for adults presenting with ALCAPA.
Author List
Selzman CH, Zimmerman MA, Campbell DNAuthor
Michael A. Zimmerman MD, FACS Professor in the Surgery department at Medical College of WisconsinMESH terms used to index this publication - Major topics in bold
AdultCoronary Vessel Anomalies
Female
Humans
Pulmonary Artery
Ventricular Function, Left
